S. Beck

发表

Alterations of the tunica vasculosa lentis in the rat model of retinopathy of prematurity

James D. Akula, Tara L. Favazza, T. Favazza, 2013, Documenta Ophthalmologica.

Implantation of ultrathin, biofunctionalized polyimide membranes into the subretinal space of rats.

S. Van Vlierberghe, P. Dubruel, S. Beck, 2011, Biomaterials.

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

S. Beck, Marina Garcia Garrido, V. Sothilingam, 2015, Nature Genetics.

Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein.

S. Beck, M. Seeliger, R. Reifen, 1999, The American journal of clinical nutrition.

Spectral domain optical coherence tomography in mouse models of retinal degeneration.

Andreas Wenzel, C. Grimm, A. Wenzel, 2009, Investigative ophthalmology & visual science.

AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2017, Front. Neurosci..

Successful Subretinal Delivery and Monitoring of MicroBeads in Mice

S. Beck, M. Seeliger, U. Wolfrum, 2013, PloS one.

A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa.

N. Tanimoto, S. Beck, M. Seeliger, 2011, Human molecular genetics.

Retina-specific activation of a sustained hypoxia-like response leads to severe retinal degeneration and loss of vision

C. Grimm, M. Samardzija, N. Tanimoto, 2011, Neurobiology of Disease.

Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies.

N. Tanimoto, S. Beck, M. Seeliger, 2010, Advances in experimental medicine and biology.

A retinal model of cerebral malaria

T. Schubert, N. Tanimoto, S. Beck, 2019, Scientific Reports.

No evidence for prooxidative effects of homocysteine in vascular endothelial cells

S. Beck, H. Biesalski, A. Flaccus, 2007, European journal of nutrition.

The absence of angiopoietin-2 leads to abnormal vascular maturation and persistent proliferative retinopathy

S. Beck, M. Seeliger, H. Hammes, 2009, Thrombosis and Haemostasis.

Mice lacking Period 1 and Period 2 circadian clock genes exhibit blue cone photoreceptor defects

N. Tanimoto, S. Beck, Christina Seide, 2013, The European journal of neuroscience.

IgA1 protease from Neisseria gonorrhoeae inhibits TNFα‐mediated apoptosis of human monocytic cells

S. Beck, T. Meyer, 2000, FEBS letters.

Influence of the β2-Subunit of L-Type Voltage-Gated Cav Channels on the Structural and Functional Development of Photoreceptor Ribbon Synapses.

S. Beck, Marina Garcia Garrido, V. Sothilingam, 2015, Investigative ophthalmology & visual science.

Multiparametric Longitudinal Profiling of RCAS-tva-Induced PDGFB-Driven Experimental Glioma

S. Beck, E. Holland, C. la Fougère, 2022, Brain sciences.

In vivo analysis of cone survival in mice.

N. Tanimoto, S. Beck, M. Seeliger, 2010, Investigative ophthalmology & visual science.

Novel Rodent Models for Macular Research

L. Peichl, C. Grimm, N. Tanimoto, 2010, PloS one.

Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy

P. Sieving, N. Tanimoto, S. Beck, 2018, The Journal of clinical investigation.

Targeted Ablation of the Pde6h Gene in Mice Reveals Cross-species Differences in Cone and Rod Phototransduction Protein Isoform Inventory*

N. Tanimoto, S. Beck, M. Seeliger, 2015, The Journal of Biological Chemistry.

Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye

N. Tanimoto, S. Beck, M. Seeliger, 2011, Development.

In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death.

C. Grimm, A. Wenzel, M. Samardzija, 2009, Human molecular genetics.

Towards a Quantitative OCT Image Analysis

Ulrich Schraermeyer, Marina Garcia Garrido, Susanne C. Beck, 2014, PloS one.

Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotype.

S. Beck, Marina Garcia Garrido, V. Sothilingam, 2015, Human molecular genetics.

PALS1 Is Essential for Retinal Pigment Epithelium Structure and Neural Retina Stratification

Till F. M. Andlauer, N. Tanimoto, S. Beck, 2011, The Journal of Neuroscience.

Crb1 is a determinant of retinal apical Müller glia cell features

S. Beck, M. Seeliger, S. A. van de Pavert, 2007, Glia.

Crb1 is a Determinant of Retinal Apical M€ uller

S. Beck, M. Seeliger, I. Versteeg, 2007 .

Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie disease

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2017, PloS one.

Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.

S. Beck, M. Seeliger, E. Zrenner, 1999, Investigative ophthalmology & visual science.

Restoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor function.

N. Tanimoto, S. Beck, M. Seeliger, 2010, Molecular therapy : the journal of the American Society of Gene Therapy.

Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa.

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2012, Human molecular genetics.

Exploring Different Serotypes And Promoters In rAAV-mediated Gene Replacement Therapy Of Achromatopsia Type 2 (ACHM2)

N. Tanimoto, S. Beck, M. Seeliger, 2011 .

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.

S. Beck, M. Knipper, B. Pichler, 2006, Brain : a journal of neurology.

Study of gene-targeted mouse models of splicing factor gene Prpf31 implicated in human autosomal dominant retinitis pigmentosa (RP).

T. Léveillard, N. Tanimoto, S. Beck, 2009, Investigative ophthalmology & visual science.

PGC-1α Determines Light Damage Susceptibility of the Murine Retina

C. Grimm, M. Samardzija, M. Okoniewski, 2012, PloS one.

Targeted Ablation of Crb1 and Crb2 in Retinal Progenitor Cells Mimics Leber Congenital Amaurosis

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2013, PLoS genetics.

Degeneration of the mouse retina upon dysregulated activity of serum response factor

S. Beck, A. Nordheim, P. Heiduschka, 2011, Molecular vision.

Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography

Andreas Wenzel, Susanne C. Beck, Mathias W. Seeliger, 2009, PloS one.

A portable albumin binder from a DNA-encoded chemical library.

Christof Baltes, Samu Melkko, Susanne C. Beck, 2008, Angewandte Chemie.

Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa.

J. Flannery, S. Beck, Marina Garcia Garrido, 2014, Human molecular genetics.

Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2013, Human molecular genetics.

Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapse.

N. Tanimoto, S. Beck, M. Seeliger, 2006, Human molecular genetics.

Endothelial SRF/MRTF ablation causes vascular disease phenotypes in murine retinae.

S. Beck, M. Seeliger, A. Nordheim, 2013, The Journal of clinical investigation.

Retinal degenerative and hypoxic ischemic disease

James D. Akula, S. Beck, R. Hansen, 2009, Documenta Ophthalmologica.

Relevance of Exocytotic Glutamate Release from Retinal Glia

T. Münch, N. Tanimoto, S. Beck, 2012, Neuron.

A reproducible and quantifiable model of choroidal neovascularization induced by VEGF A165 after subretinal adenoviral gene transfer in the rabbit

S. Beck, P. Heiduschka, S. Kochanek, 2008, Molecular vision.

In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopy

Andreas Wenzel, Eberhart Zrenner, Susanne C. Beck, 2005, Vision Research.

Loss of CRB 2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB 1 gene

N. Tanimoto, S. Beck, M. Seeliger, 2012 .

Title Targeted ablation of Crb 2 in photoreceptor cells induces retinitis pigmentosa

J. Flannery, S. Beck, Christina Seide, 2014 .

In vivo assessment of retinal vascular wall dimensions.

Birgit Lorenz, Yuxi Feng, Christoph Kernstock, 2010, Investigative ophthalmology & visual science.

Cooperative phagocytes: resident microglia and bone marrow immigrants remove dead photoreceptors in retinal lesions.

C. Grimm, M. Samardzija, C. Remé, 2009, The American journal of pathology.

A retinal model of cerebral malaria

T. Schubert, N. Tanimoto, S. Beck, 2019, Scientific Reports.

Uptake and nuclear transport of Neisseria IgA1 protease‐associated α‐proteins in human cells

S. Beck, T. Meyer, Susanne C Beck, 1995, Molecular microbiology.

Contribution of the hexosamine biosynthetic pathway in the hyperglycemia-dependent and -independent breakdown of the retinal neurovascular unit

T. Wieland, S. Beck, H. Hammes, 2023, Molecular metabolism.

Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa.

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2014, Advances in experimental medicine and biology.

Murine Autoimmune Optic Neuritis Is Not Phenotypically Altered by the Retinal Degeneration 8 Mutation.

Ricarda Diem, Sarah K Williams, Veit Flockerzi, 2017, Investigative ophthalmology & visual science.

Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina

S. Beck, Marina Garcia Garrido, V. Sothilingam, 2018, Scientific Reports.

Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsia.

N. Tanimoto, S. Beck, M. Seeliger, 2012, Advances in experimental medicine and biology.

Elk3 Deficiency Causes Transient Impairment in Post-Natal Retinal Vascular Development and Formation of Tortuous Arteries in Adult Murine Retinae

S. Beck, Marina Garcia Garrido, V. Sothilingam, 2014, PloS one.

Scale Adjustments to Facilitate Two-Dimensional Measurements in OCT Images

Marina Garcia Garrido, Regine L. Mühlfriedel, Susanne C. Beck, 2015, PloS one.

Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei

N. Tanimoto, S. Beck, D. Hicks, 2010, Neuroscience.